Global Variome shared LOVD

LOVD v.3.0 Build 30b [ Current LOVD status ] Register as submitter | Log in

Phenotype #0000281826 Individual ID 00388271 Associated disease PMC Phenotype details Myotonia, clinically paramyotonia congenita, daughter with similar syptomatics Diagnosis/Initial - Inheritance Familial, autosomal dominant Diagnosis/Definite - Age/Examination 46y (46 years) Age/Diagnosis - Age/Onset - Phenotype/Onset - Protein - Owner name Andreas Laner Database submission license Creative Commons Attribution 4.0 International Created by Andreas Laner Date created 2021-11-03 14:24:24 +01:00 (CET) Date last edited 2021-11-03 14:34:32 +01:00 (CET)

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